Jueun Kim, Donghyeon Kim, Byung Gwan Park, Daewon Oh, Shinjae Lee, Jihun Kim, Eonu Nam and Kwangjin An
{"title":"Effective production of liquid/wax fuels from polyethylene plastics using Ru/Al2O3 catalysts†","authors":"Jueun Kim, Donghyeon Kim, Byung Gwan Park, Daewon Oh, Shinjae Lee, Jihun Kim, Eonu Nam and Kwangjin An","doi":"10.1039/D5EY00070J","DOIUrl":null,"url":null,"abstract":"<p >Hydrogenolysis provides a promising pathway for converting polyolefin plastics into valuable liquid and wax fuels. This process involves dehydrogenation, C–C bond cleavage, and hydrogenation at the active metal sites of the catalyst. Controlling the nature of these metal sites is crucial to optimize overall reaction activity. In this study, Ru catalysts supported on nanosheet-assembled Al<small><sub>2</sub></small>O<small><sub>3</sub></small> (NA-Al<small><sub>2</sub></small>O<small><sub>3</sub></small>) were used for the hydrogenolysis of polyethylene (PE). Unlike commercial Al<small><sub>2</sub></small>O<small><sub>3</sub></small>, NA-Al<small><sub>2</sub></small>O<small><sub>3</sub></small> promotes Ru–Al bond formation, leading to stronger metal–support interactions. Under identical Ru loadings, these enhanced interactions resulted in higher Ru dispersion and smaller Ru species on the NA-Al<small><sub>2</sub></small>O<small><sub>3</sub></small> surface. To investigate the effect of Ru loading, a series of catalysts (<em>x</em>Ru/NA-Al<small><sub>2</sub></small>O<small><sub>3</sub></small>, <em>x</em> = 0.5, 1, 5, and 8 wt% Ru) was synthesized, revealing that Ru particle size and electronic properties varied with Ru loading. Among them, the 1Ru/NA-Al<small><sub>2</sub></small>O<small><sub>3</sub></small> catalyst, featuring optimally sized Ru species (∼0.8 nm) and a tailored electronic structure, demonstrated the highest efficiency in PE hydrogenolysis by effectively suppressing successive C–C bond cleavage. This catalyst achieved an outstanding PE conversion rate of 1.15 × 10<small><sup>3</sup></small> g<small><sub>converted PE</sub></small> g<small><sub>Ru</sub></small><small><sup>−1</sup></small> h<small><sup>−1</sup></small> and a liquid/wax production rate of 9.23 x 10<small><sup>2</sup></small> g<small><sub>liquid/wax</sub></small> g<small><sub>Ru</sub></small><small><sup>−1</sup></small> h<small><sup>−1</sup></small>, highlighting its superior performance in catalytic PE hydrogenolysis.</p>","PeriodicalId":72877,"journal":{"name":"EES catalysis","volume":" 4","pages":" 822-831"},"PeriodicalIF":0.0000,"publicationDate":"2025-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/ey/d5ey00070j?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"EES catalysis","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ey/d5ey00070j","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Hydrogenolysis provides a promising pathway for converting polyolefin plastics into valuable liquid and wax fuels. This process involves dehydrogenation, C–C bond cleavage, and hydrogenation at the active metal sites of the catalyst. Controlling the nature of these metal sites is crucial to optimize overall reaction activity. In this study, Ru catalysts supported on nanosheet-assembled Al2O3 (NA-Al2O3) were used for the hydrogenolysis of polyethylene (PE). Unlike commercial Al2O3, NA-Al2O3 promotes Ru–Al bond formation, leading to stronger metal–support interactions. Under identical Ru loadings, these enhanced interactions resulted in higher Ru dispersion and smaller Ru species on the NA-Al2O3 surface. To investigate the effect of Ru loading, a series of catalysts (xRu/NA-Al2O3, x = 0.5, 1, 5, and 8 wt% Ru) was synthesized, revealing that Ru particle size and electronic properties varied with Ru loading. Among them, the 1Ru/NA-Al2O3 catalyst, featuring optimally sized Ru species (∼0.8 nm) and a tailored electronic structure, demonstrated the highest efficiency in PE hydrogenolysis by effectively suppressing successive C–C bond cleavage. This catalyst achieved an outstanding PE conversion rate of 1.15 × 103 gconverted PE gRu−1 h−1 and a liquid/wax production rate of 9.23 x 102 gliquid/wax gRu−1 h−1, highlighting its superior performance in catalytic PE hydrogenolysis.